| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000351677 |
| Start |
112504709:112504709(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1727G>T |
| AA Mutation |
p.Ser576Ile(p.S576I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000351677 |
| Start |
112473023:112473023(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs121918456
|
| CDS Mutation |
c.836A>G |
| AA Mutation |
p.Tyr279Cys(p.Y279C) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
4 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000351677 |
| Start |
112477910:112477910(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.987C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |